Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Dr.MUSIC 3s

K-Number: K172451 · 2017-11-17

ApplicantSmartmedicaldevice Co., Ltd.
Decision Date2017-11-17
Product CodeNUH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Dr.MUSIC 3s is a medical device manufactured by Smartmedicaldevice Co., Ltd.. It received FDA 510(k) clearance on 2017-11-17 under approval number K172451. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Dr.MUSIC 3s?

Dr.MUSIC 3s is a medical device that received FDA 510(k) clearance on 2017-11-17. It is manufactured by Smartmedicaldevice Co., Ltd.. The 510(k) number is K172451.

When was Dr.MUSIC 3s approved by the FDA?

Dr.MUSIC 3s received FDA 510(k) clearance on 2017-11-17, under approval number K172451.

What company makes Dr.MUSIC 3s?

Dr.MUSIC 3s is manufactured by Smartmedicaldevice Co., Ltd..

What is the FDA product code for Dr.MUSIC 3s?

The FDA product code for Dr.MUSIC 3s is NUH.

Related Devices (Code: NUH)

K162630CP Relief Wand-OTCMid-America Medical Innovations, LLC K161453WELL LIFE Wireless TENS/EMS Stimulator, Models WR-2605/2605AWell-Life Healthcare Limited K160508Electronic Pulse StimulatorBeijing Choice Electronic Technololgy Co., Ltd. K161537OTC TENS Device, Model PTS-IVCounter Scientific Development (Gz), Ltd. K151995Painmaster MCT PatchNewmark, Inc. K160255HBOTC Muscle and Nerve StimulatorHb Medical, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑